Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,3,3-Triiodoallyl-p-toluenesulfonate | HCID 13233003 | — |
| Reactant | HCID 20252102 | HCID 20252102 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 497093 | HCID 497093 | — |
Reaction Steps
To a solution of 104 mg (0.5 mmoles) of 2,3-dichloro-4-ethoxycarbonylpyrrole in 5 ml of dry N,N-dimethylformamide were added 303 mg (0.5 mmoles) of 2,3,3-triiodoallyl-p-toluenesulfonate and 0.07 ml (0.5 mmoles) of triethylamine and the resulting mixture was heated at 60° C. for 2 hours. The reaction mixture was cooled, 10 ml of cold water were added with stirring thereto and the so separated crystalline substance, 1-(2',3',3'-triiodoallyl)-2,3-dichloro-4-ethyoxycarbonylpyrrole, was recovered by filtration, washed with water and then dried. Yield 281 mg (90%), mp 117°-119° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04563472 |
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| Source dataset | uspto-grants-1986_01 |
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| ORD ID | ord-d3dc4a754e764a2ba13e91a3629d87c3 |
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| Source note | uspto-grants-1986_01 |
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